{"count":220695,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=133","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=131","results":[{"created":"2025-11-14T13:00:13.005509+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"1.28","user_name":"Chirag Patel","item_type":"entity","text":"Publications for gene: AP1S1 were set to PMID: 32306098","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:59:46.074053+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.269","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: AP1S1 were changed from MEDNIK syndrome 609313; non-syndromic congenital intestinal failure to MEDNIK syndrome, MONDO:0012251","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:59:43.250981+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"1.27","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: AP1S1 as Green List (high evidence)","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:59:43.242779+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"1.27","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ap1s1 has been classified as Green List (High Evidence).","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:59:31.135969+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.269","user_name":"Chirag Patel","item_type":"entity","text":"Publications for gene: AP1S1 were set to 32306098","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:58:53.826390+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.268","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: AP1S1 as ready","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:58:53.815555+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.268","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ap1s1 has been classified as Green List (High Evidence).","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:58:01.088113+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.268","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene AP1S1 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-14T12:58:00.915526+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.268","user_name":"Chirag Patel","item_type":"entity","text":"gene: AP1S1 was added\ngene: AP1S1 was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AP1S1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1S1 were set to 32306098\nPhenotypes for gene: AP1S1 were set to MEDNIK syndrome 609313; non-syndromic congenital intestinal failure","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:57:22.100620+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"1.26","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene AP1S1 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2025-11-14T12:54:25.448510+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3549","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: AP1S1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19057675, 23423674, 30244301, 32306098, 24754424, 39541497; Phenotypes: MEDNIK syndrome, MONDO:0012251; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"AP1S1","entity_type":"gene"},{"created":"2025-11-14T12:48:59.412869+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.267","user_name":"Chirag Patel","item_type":"entity","text":"Publications for gene: TUBB4B were set to 31884617, 38662826, 37448631, 35240325, 38719929, 39876836, 29198720","entity_name":"TUBB4B","entity_type":"gene"},{"created":"2025-11-14T12:48:45.737899+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.267","user_name":"Chirag Patel","item_type":"entity","text":"Publications for gene: TUBB4B were set to 31884617, 38662826, 37448631, 35240325, 38719929, 39876836, 29198720","entity_name":"TUBB4B","entity_type":"gene"},{"created":"2025-11-14T12:48:03.238158+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.266","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: TUBB4B were changed from Leber congenital amaurosis with early-onset deafness, MIM#\t617879 to TUBB4B-related ciliopathy, MONDO:1060115","entity_name":"TUBB4B","entity_type":"gene"},{"created":"2025-11-14T12:47:49.428009+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.266","user_name":"Chirag Patel","item_type":"entity","text":"Publications for gene: TUBB4B were set to 29198720","entity_name":"TUBB4B","entity_type":"gene"},{"created":"2025-11-14T12:47:16.150722+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.265","user_name":"Chirag Patel","item_type":"entity","text":"edited their review of gene: TUBB4B: Added comment: ClinGen definitive gene-disease association.\r\nAffected individuals also exhibited congenital or childhood onset sensorineural hearing impairment.; Changed publications: 31884617, 38662826, 37448631, 35240325, 38719929, 39876836, 29198720; Changed phenotypes: TUBB4B-related ciliopathy, MONDO:1060115","entity_name":"TUBB4B","entity_type":"gene"},{"created":"2025-11-14T12:44:43.337754+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.265","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: TRPV4 were changed from Auditory neuropathy spectrum disorder; Peripheral neuropathy; Hearing loss to Auditory neuropathy spectrum disorder; Charcot-Marie-Tooth disease axonal type 2C, MONDO:0011633; Hearing loss","entity_name":"TRPV4","entity_type":"gene"},{"created":"2025-11-14T12:44:01.949809+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.264","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TRPV4: Rating: GREEN; Mode of pathogenicity: None; Publications: 20037586; Phenotypes: Charcot-Marie-Tooth disease axonal type 2C, MONDO:0011633; Mode of inheritance: None","entity_name":"TRPV4","entity_type":"gene"},{"created":"2025-11-14T12:36:33.963935+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.264","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: TMEM132E as Red List (low evidence)","entity_name":"TMEM132E","entity_type":"gene"},{"created":"2025-11-14T12:36:33.955613+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.264","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tmem132e has been classified as Red List (Low Evidence).","entity_name":"TMEM132E","entity_type":"gene"},{"created":"2025-11-14T12:31:46.309807+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.263","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PSMC3 as Green List (high evidence)","entity_name":"PSMC3","entity_type":"gene"},{"created":"2025-11-14T12:31:46.299240+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.263","user_name":"Chirag Patel","item_type":"entity","text":"Gene: psmc3 has been classified as Green List (High Evidence).","entity_name":"PSMC3","entity_type":"gene"},{"created":"2025-11-14T12:31:27.195675+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.262","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PSMC3: Rating: GREEN; Mode of pathogenicity: None; Publications: 37256937; Phenotypes: Neurodevelopmental disorder, MONDO:0700092, PSMC3-related; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PSMC3","entity_type":"gene"},{"created":"2025-11-14T12:27:43.988347+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.262","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PAX2 as Green List (high evidence)","entity_name":"PAX2","entity_type":"gene"},{"created":"2025-11-14T12:27:43.978588+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.262","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pax2 has been classified as Green List (High Evidence).","entity_name":"PAX2","entity_type":"gene"},{"created":"2025-11-14T12:27:22.835540+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.261","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PAX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 22213154; Phenotypes: Renal coloboma syndrome, MONDO:0007352; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PAX2","entity_type":"gene"},{"created":"2025-11-14T11:37:45.966675+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.261","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: DSPP as Green List (high evidence)","entity_name":"DSPP","entity_type":"gene"},{"created":"2025-11-14T11:37:45.956427+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.261","user_name":"Chirag Patel","item_type":"entity","text":"Gene: dspp has been classified as Green List (High Evidence).","entity_name":"DSPP","entity_type":"gene"},{"created":"2025-11-14T11:37:14.560377+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: DSPP: Rating: GREEN; Mode of pathogenicity: None; Publications: 11175790, 15690376, 17686168, 15592686, 18456718, 15241678; Phenotypes: Dentinogenesis imperfecta, MONDO:0018849; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DSPP","entity_type":"gene"},{"created":"2025-11-14T11:23:55.134381+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: ADAMTS1 as ready","entity_name":"ADAMTS1","entity_type":"gene"},{"created":"2025-11-14T11:23:55.098604+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: adamts1 has been classified as Red List (Low Evidence).","entity_name":"ADAMTS1","entity_type":"gene"},{"created":"2025-11-14T11:23:39.699608+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: ANKRD24 as ready","entity_name":"ANKRD24","entity_type":"gene"},{"created":"2025-11-14T11:23:39.684777+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ankrd24 has been classified as Red List (Low Evidence).","entity_name":"ANKRD24","entity_type":"gene"},{"created":"2025-11-14T11:23:32.539533+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: ATP11A as ready","entity_name":"ATP11A","entity_type":"gene"},{"created":"2025-11-14T11:23:32.532219+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: atp11a has been classified as Green List (High Evidence).","entity_name":"ATP11A","entity_type":"gene"},{"created":"2025-11-14T11:23:20.491346+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CPD as ready","entity_name":"CPD","entity_type":"gene"},{"created":"2025-11-14T11:23:20.484184+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: cpd has been classified as Green List (High Evidence).","entity_name":"CPD","entity_type":"gene"},{"created":"2025-11-14T11:23:09.775047+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: GOSR2 as ready","entity_name":"GOSR2","entity_type":"gene"},{"created":"2025-11-14T11:23:09.767464+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: gosr2 has been classified as Red List (Low Evidence).","entity_name":"GOSR2","entity_type":"gene"},{"created":"2025-11-14T11:22:59.623297+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: IKZF2 as ready","entity_name":"IKZF2","entity_type":"gene"},{"created":"2025-11-14T11:22:59.612428+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ikzf2 has been classified as Green List (High Evidence).","entity_name":"IKZF2","entity_type":"gene"},{"created":"2025-11-14T11:22:50.826901+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MEPE as ready","entity_name":"MEPE","entity_type":"gene"},{"created":"2025-11-14T11:22:50.819486+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: mepe has been classified as Amber List (Moderate Evidence).","entity_name":"MEPE","entity_type":"gene"},{"created":"2025-11-14T11:22:41.677756+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MPDZ as ready","entity_name":"MPDZ","entity_type":"gene"},{"created":"2025-11-14T11:22:41.667332+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: mpdz has been classified as Red List (Low Evidence).","entity_name":"MPDZ","entity_type":"gene"},{"created":"2025-11-14T11:22:32.492128+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: NCOA3 as ready","entity_name":"NCOA3","entity_type":"gene"},{"created":"2025-11-14T11:22:32.483952+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ncoa3 has been classified as Red List (Low Evidence).","entity_name":"NCOA3","entity_type":"gene"},{"created":"2025-11-14T10:30:36.048628+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: REST as ready","entity_name":"REST","entity_type":"gene"},{"created":"2025-11-14T10:30:36.037905+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: rest has been classified as Amber List (Moderate Evidence).","entity_name":"REST","entity_type":"gene"},{"created":"2025-11-14T10:30:27.590123+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SEZ6 as ready","entity_name":"SEZ6","entity_type":"gene"},{"created":"2025-11-14T10:30:27.581787+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: sez6 has been classified as Red List (Low Evidence).","entity_name":"SEZ6","entity_type":"gene"},{"created":"2025-11-14T10:30:17.832051+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SMARCA4 as ready","entity_name":"SMARCA4","entity_type":"gene"},{"created":"2025-11-14T10:30:17.824523+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: smarca4 has been classified as Red List (Low Evidence).","entity_name":"SMARCA4","entity_type":"gene"},{"created":"2025-11-14T10:30:04.565978+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TECTB as ready","entity_name":"TECTB","entity_type":"gene"},{"created":"2025-11-14T10:30:04.554849+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tectb has been classified as Red List (Low Evidence).","entity_name":"TECTB","entity_type":"gene"},{"created":"2025-11-14T10:29:53.868174+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TRRAP as ready","entity_name":"TRRAP","entity_type":"gene"},{"created":"2025-11-14T10:29:53.858357+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: trrap has been classified as Red List (Low Evidence).","entity_name":"TRRAP","entity_type":"gene"},{"created":"2025-11-14T10:29:44.355146+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CENPP as ready","entity_name":"CENPP","entity_type":"gene"},{"created":"2025-11-14T10:29:44.347520+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: cenpp has been classified as Red List (Low Evidence).","entity_name":"CENPP","entity_type":"gene"},{"created":"2025-11-14T10:29:35.618564+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MAP3K1 as ready","entity_name":"MAP3K1","entity_type":"gene"},{"created":"2025-11-14T10:29:35.608673+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: map3k1 has been classified as Red List (Low Evidence).","entity_name":"MAP3K1","entity_type":"gene"},{"created":"2025-11-14T10:29:25.773420+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TOGARAM2 as ready","entity_name":"TOGARAM2","entity_type":"gene"},{"created":"2025-11-14T10:29:25.763690+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: togaram2 has been classified as Red List (Low Evidence).","entity_name":"TOGARAM2","entity_type":"gene"},{"created":"2025-11-14T10:29:16.848631+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: STX4 as ready","entity_name":"STX4","entity_type":"gene"},{"created":"2025-11-14T10:29:16.841091+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: stx4 has been classified as Amber List (Moderate Evidence).","entity_name":"STX4","entity_type":"gene"},{"created":"2025-11-14T10:29:05.411617+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MVD as ready","entity_name":"MVD","entity_type":"gene"},{"created":"2025-11-14T10:29:05.403803+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: mvd has been classified as Red List (Low Evidence).","entity_name":"MVD","entity_type":"gene"},{"created":"2025-11-14T10:28:57.261745+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: PKHD1L1 as ready","entity_name":"PKHD1L1","entity_type":"gene"},{"created":"2025-11-14T10:28:57.250389+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pkhd1l1 has been classified as Green List (High Evidence).","entity_name":"PKHD1L1","entity_type":"gene"},{"created":"2025-11-14T10:28:43.492908+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: FXN as ready","entity_name":"FXN","entity_type":"gene"},{"created":"2025-11-14T10:28:43.482799+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: fxn has been classified as Green List (High Evidence).","entity_name":"FXN","entity_type":"gene"},{"created":"2025-11-14T10:28:33.504486+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MPZ as ready","entity_name":"MPZ","entity_type":"gene"},{"created":"2025-11-14T10:28:33.496685+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: mpz has been classified as Red List (Low Evidence).","entity_name":"MPZ","entity_type":"gene"},{"created":"2025-11-14T10:28:23.659047+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: PCDH9 as ready","entity_name":"PCDH9","entity_type":"gene"},{"created":"2025-11-14T10:28:23.649131+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pcdh9 has been classified as Red List (Low Evidence).","entity_name":"PCDH9","entity_type":"gene"},{"created":"2025-11-14T10:27:48.654355+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TMEM126A as ready","entity_name":"TMEM126A","entity_type":"gene"},{"created":"2025-11-14T10:27:48.646485+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tmem126a has been classified as Amber List (Moderate Evidence).","entity_name":"TMEM126A","entity_type":"gene"},{"created":"2025-11-14T10:27:20.748723+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: NEFL as ready","entity_name":"NEFL","entity_type":"gene"},{"created":"2025-11-14T10:27:20.738125+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"entity","text":"Gene: nefl has been classified as Green List (High Evidence).","entity_name":"NEFL","entity_type":"gene"},{"created":"2025-11-14T09:50:53.190840+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.260","user_name":"Chirag Patel","item_type":"panel","text":"HPO terms changed from Hearing impairment, HP:0000365 to Hearing impairment, HP:0000365; Sensorineural hearing impairment HP:0000407","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:30:29.460563+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.259","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene NEFL from panel Auditory Neuropathy","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:30:29.161836+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.259","user_name":"Chirag Patel","item_type":"entity","text":"gene: NEFL was added\ngene: NEFL was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Literature\nMode of inheritance for gene: NEFL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NEFL were set to 21176974\nPhenotypes for gene: NEFL were set to Syndromic auditory neuropathy spectrum disorder","entity_name":"NEFL","entity_type":"gene"},{"created":"2025-11-14T09:28:50.092523+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.258","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene TMEM126A from panel Auditory Neuropathy","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:28:49.910611+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.258","user_name":"Chirag Patel","item_type":"entity","text":"gene: TMEM126A was added\ngene: TMEM126A was added to Deafness_IsolatedAndComplex. Sources: Expert Review Amber,Literature\nMode of inheritance for gene: TMEM126A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TMEM126A were set to 21176974\nPhenotypes for gene: TMEM126A were set to Optic atrophy 7 MIM#612989; Syndromic auditory neuropathy spectrum disorder","entity_name":"TMEM126A","entity_type":"gene"},{"created":"2025-11-14T09:27:36.335843+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.257","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PMP22 as Green List (high evidence)","entity_name":"PMP22","entity_type":"gene"},{"created":"2025-11-14T09:27:36.325235+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.257","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pmp22 has been classified as Green List (High Evidence).","entity_name":"PMP22","entity_type":"gene"},{"created":"2025-11-14T09:27:19.249838+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.257","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PMP22 as Green List (high evidence)","entity_name":"PMP22","entity_type":"gene"},{"created":"2025-11-14T09:27:19.227684+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.257","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pmp22 has been classified as Green List (High Evidence).","entity_name":"PMP22","entity_type":"gene"},{"created":"2025-11-14T09:26:48.372708+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.256","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene PCDH9 from panel Auditory Neuropathy","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:26:48.147869+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.256","user_name":"Chirag Patel","item_type":"entity","text":"gene: PCDH9 was added\ngene: PCDH9 was added to Deafness_IsolatedAndComplex. Sources: Expert Review Red,Literature\nMode of inheritance for gene: PCDH9 was set to Unknown\nPublications for gene: PCDH9 were set to 21176974\nPhenotypes for gene: PCDH9 were set to Non-syndromic auditory neuropathy spectrum disorder","entity_name":"PCDH9","entity_type":"gene"},{"created":"2025-11-14T09:26:08.907437+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.255","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene MPZ from panel Auditory Neuropathy","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:26:08.691786+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.255","user_name":"Chirag Patel","item_type":"entity","text":"gene: MPZ was added\ngene: MPZ was added to Deafness_IsolatedAndComplex. Sources: Expert Review Red,Literature\nMode of inheritance for gene: MPZ was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: MPZ were set to 21176974; 12845552; 12805115\nPhenotypes for gene: MPZ were set to Syndromic auditory neuropathy spectrum disorder","entity_name":"MPZ","entity_type":"gene"},{"created":"2025-11-14T09:25:32.534518+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.255","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene FXN from panel Auditory Neuropathy","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:25:32.364310+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.255","user_name":"Chirag Patel","item_type":"entity","text":"gene: FXN was added\ngene: FXN was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Literature\nSTR tags were added to gene: FXN.\nMode of inheritance for gene: FXN was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FXN were set to 18515321; 25791504\nPhenotypes for gene: FXN were set to Friedreich ataxia MIM#229300","entity_name":"FXN","entity_type":"gene"},{"created":"2025-11-14T09:23:38.066593+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.254","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene PKHD1L1 from panel Deafness_Isolated","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:23:37.896894+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.254","user_name":"Chirag Patel","item_type":"entity","text":"gene: PKHD1L1 was added\ngene: PKHD1L1 was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Literature\nMode of inheritance for gene: PKHD1L1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PKHD1L1 were set to 38459354\nPhenotypes for gene: PKHD1L1 were set to non syndromic hearing loss (MONDO:0020678)","entity_name":"PKHD1L1","entity_type":"gene"},{"created":"2025-11-14T09:21:25.772314+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.253","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene MVD from panel Deafness_Isolated","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:21:25.586927+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.253","user_name":"Chirag Patel","item_type":"entity","text":"gene: MVD was added\ngene: MVD was added to Deafness_IsolatedAndComplex. Sources: Expert Review Red,Literature\nMode of inheritance for gene: MVD was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MVD were set to 34135477\nPhenotypes for gene: MVD were set to Nonsyndromic genetic hearing loss MONDO:0019497, MPDZ-related","entity_name":"MVD","entity_type":"gene"},{"created":"2025-11-14T09:20:49.772359+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.252","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene STX4 from panel Deafness_Isolated","entity_name":null,"entity_type":null},{"created":"2025-11-14T09:20:49.510187+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.252","user_name":"Chirag Patel","item_type":"entity","text":"gene: STX4 was added\ngene: STX4 was added to Deafness_IsolatedAndComplex. Sources: Expert Review Amber,Literature\nMode of inheritance for gene: STX4 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STX4 were set to 36355422\nPhenotypes for gene: STX4 were set to Deafness, autosomal recessive 123, MIM# 620745","entity_name":"STX4","entity_type":"gene"}]}